Food Recall Check
Class I · High risk Terminated Initiated Mar 20, 2018 (9 years ago)

Bloody Hell Mary recall

Recalled by Kitchen By The Sea · Panama City Beach, FL, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

allergen warning not listed on labels , egg, soy and wheat including sulfites

Undeclared allergens: Egg Soy Wheat

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Bloody Hell Mary, HOT, Kitchen By The Sea, From the Beach House, Net Wt. 32 oz. (.9L), Low Sodium

Quantity: 11 quarts (352 ounces)

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

BM Batch # 41B19217A,41B21517A,41B26117A,41B29817A,41B32617A,41B34817A

Where it was sold

FDA's distribution note: U.S. consignees only.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to egg, soy, wheat; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Kitchen By The Sea
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 20, 2018
In FDA report of
May 2, 2018
Terminated
Sep 17, 2019
FDA recall number
F-1137-2018 · event 79675
Official record
FDA enforcement report search

Also recalled with it (1 more product)

FDA files each product of one recall action separately; these share the same FDA event.